Early Exercise Efforts in Multiple Sclerosis
Primary Purpose
Multiple Sclerosis
Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Systematic exercise training
Educational program
Sponsored by

About this trial
This is an interventional treatment trial for Multiple Sclerosis focused on measuring Multiple sclerosis, Exercise, Disease-modifying treatment, Early treatment
Eligibility Criteria
Inclusion Criteria:
- Signed consent
- Definite diagnosis with Relapsing remitting multiple sclerosis (RRMS)
- No more than 2 years since diagnosis
- Expectedly able to carry out high intensity aerobic training
- Able to transport themselves to and from training sessions
Exclusion Criteria:
- Pregnancy
- Dementia, alcohol abuse, or pacemaker
- Metallic implants, hindering MRI-scans
- Comorbidities hindering participation in high intensity aerobic training
Sites / Locations
- Section for Sport Science, Department of Public Health, University of Aarhus
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Active Comparator
No Intervention
Arm Label
Systematic exercise training
Educational program
Standard treatment alone
Arm Description
Two weekly supervised aerobic exercise trainings for 48 weeks. The training will be planned by exercise physiologists, and performed in a progressive manner.
Educational program on physical activity and health, consisting of four educational sessions in the intervention period.
Data from The Danish MS Registry will serve as control-data for standard treatment alone.
Outcomes
Primary Outcome Measures
Change in Annual Relapse Rate (ARR)
Number of relapses, registered and validated by neurologist, on annual basis
Percentage brain volume change
Brain atrophy will be measured from MRI-scans
Secondary Outcome Measures
Multiple Sclerosis Functional Composite (MSFC)
Composite score from Timed 25-Feet Walk Test (T25FWT), 9-Hole Peg Test (9HPT), Paced Auditory Serial Addition Test (PASAT)
Expanded Disability Status Scale (EDSS) score
Disability status score assessed and registered by neurologist. The scale ranges from 0-10 in 0.5 unit increments representing higher levels of disability.
Full Information
NCT ID
NCT03322761
First Posted
October 16, 2017
Last Updated
November 2, 2022
Sponsor
University of Aarhus
Collaborators
University of Southern Denmark, Region of Southern Denmark
1. Study Identification
Unique Protocol Identification Number
NCT03322761
Brief Title
Early Exercise Efforts in Multiple Sclerosis
Official Title
Exercise as a Supplemental Treatment Strategy Early in the Disease Course of Multiple Sclerosis
Study Type
Interventional
2. Study Status
Record Verification Date
February 2021
Overall Recruitment Status
Completed
Study Start Date
April 1, 2018 (Actual)
Primary Completion Date
December 31, 2021 (Actual)
Study Completion Date
December 31, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Aarhus
Collaborators
University of Southern Denmark, Region of Southern Denmark
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This study seeks to investigate whether early exercise efforts can expand the use of exercise in Multiple sclerosis (MS), from symptom treatment only, to early supplementary disease-modifying treatment.
The study will be conducted in a randomized and controlled manner, with single blinding. Participants will be allocated to either a systematic aerobic exercise intervention or an educational programme on exercise and physical activity. Both interventions will last 1 year, and involve a 1 year follow-up period.
It is hypothesized that early exercise efforts can modify the disease activity and disability progression.
Detailed Description
Multiple Sclerosis (MS) is an autoimmune and neurodegenerative disease in the central nervous system (CNS), characterized by a complex pathogenesis and heterogeneous symptoms. The histopathological hallmark of the disease is sclerotic lesions. These inflammatory lesions manifests as disabling relapses, and the number of relapses in the first few years after disease onset is associated with progression of disability, with a higher number of relapses leading to a more rapid progression. In addition, diffuse neurodegeneration seems to occur early in the disease, and even though it is not always clinically evident it is associated with disease progression. A reduction in relapse rate and neurodegeneration early in the MS disease course may slow the progression of disabilities and can possibly reduce overall disease burden. For the individual person with MS (pwMS) a reduction in overall disease burden will often improve quality of life, and since MS is a lifelong disease this is of great interest. Preventing disability in pwMS is also highly relevant in a societal perspective, as it lowers the large costs associated with increased disability. As a consequence, the importance of early treatment have been emphasized.
Treatment of MS have seen great advances in the recent years, resulting in an increasing number of available disease-modifying treatments (DMT). Despite the fact that the current DMTs favourable alter a number of clinical outcomes and the course of the disease, it is still a serious and deteriorating condition with significant disease activity, impaired neurological functions and thus progression of disabilities. New and supplemental treatment strategies are therefore still warranted, and exercise have gained attention as a safe and tolerable rehabilitation strategy. Recently, exercise furthermore have gained substantial attention, as the first indications of neuroprotective and disease-modifying effects of exercise has been published. However, despite the focus on early treatment in medical DMTs no studies have investigated the effects of exercise as a supplemental treatment strategy early in the disease course of MS.
Consequently, the purpose of this study is to investigate the effects of early exercise efforts on disease activity and disability progression. In a sub-group the effects will furthermore be investigated on brain volume, specific brain regions, and inflammation.
It is hypothesized that early exercise efforts can modify the disease activity and disability progression, by reducing the relapse rate, the progression of Multiple Sclerosis Functional Composite (MSFC) and Expanded Disability Status Scale (EDSS) scores. The rate of brain atrophy and the lesion load, obtained by MRI scans, is also hypothesized to be reduced. This is expected to be due to an exercise-induced reduction in inflammation.
The study will be a randomised and controlled study with randomisation to either an systematic aerobic exercise intervention or an educational programme on exercise and physical activity. Both interventions are in addition to standard treatment, and will last 1 year. The exercise intervention will consist of 2 supervised exercise sessions per week in the complete duration of the study, while the standard treatment plus exercise education program will consist of 4 educational sessions on the health benefits associated with exercise and physical activity held every third month throughout the intervention period. The training in the exercise group will be aerobic exercise (running, cycling, rowing or on a cross-trainer) planned by exercise physiologists and performed in a progressive manner. To allow handling of a large number of participants, who is also geographically spread, the exercise intervention will be locally anchored, but at the same time supervised by student employees from Section for Sports Science and controlled by internet- and telephonic communication. In addition to the two intervention groups, data from The Danish MS registry will serve as population based standard treatment control data. All groups will be followed up 1 year after cessation of the interventions.
To set the estimated number of participants a two-sample two-sided power calculation has been conducted. The basis for this calculation is an report from Tallner et al. who have shown a difference in relapse rate during a two-year period (equal to our 1 year intervention, and 1 year follow-up) of 0.65 relapses between physically active and physically inactive MS patients (active: 0.95 +/- 0.97 relapses in 2 years ; inactive: 1.60 +/- 1.64 relapses in 2 years). 83 patients with MS should be enrolled in each intervention group (a 20% drop-out rate has been included). Newly published data on the brain atrophy in percentage of total brain volume after 24 weeks of resistance training have been the basis for a similar calculation of the number of participants in the sub-group, from whom MRI-scans and blood samples will be obtained. 41 participants from each intervention group should form this sub-group.
MS is a complex disease with heterogenous symptoms, and by combining the disciplines of exercise physiology, neurology and radiology this study can be the first long-term and large-scale exercise study to investigate the possible neuroprotective and disease-modifying effects of exercise when initiated early in the disease course of MS. Consequently, this project has the potential to change present clinical practice and generate further attention to exercise, not only as symptom treatment, but also as an supplemental disease-modifying treatment strategy early in the course of MS.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple Sclerosis
Keywords
Multiple sclerosis, Exercise, Disease-modifying treatment, Early treatment
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
84 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Systematic exercise training
Arm Type
Experimental
Arm Description
Two weekly supervised aerobic exercise trainings for 48 weeks. The training will be planned by exercise physiologists, and performed in a progressive manner.
Arm Title
Educational program
Arm Type
Active Comparator
Arm Description
Educational program on physical activity and health, consisting of four educational sessions in the intervention period.
Arm Title
Standard treatment alone
Arm Type
No Intervention
Arm Description
Data from The Danish MS Registry will serve as control-data for standard treatment alone.
Intervention Type
Combination Product
Intervention Name(s)
Systematic exercise training
Intervention Description
Combination of standard medical treatment and systematic early exercise training in persons with MS.
Intervention Type
Behavioral
Intervention Name(s)
Educational program
Intervention Description
Informations regarding health benefits of physical activity and exercise.
Primary Outcome Measure Information:
Title
Change in Annual Relapse Rate (ARR)
Description
Number of relapses, registered and validated by neurologist, on annual basis
Time Frame
ARR, 1 year intervention; 1 year follow up.
Title
Percentage brain volume change
Description
Brain atrophy will be measured from MRI-scans
Time Frame
Baseline, 24 weeks, after 1 year intervention, and again at 1 year follow up.
Secondary Outcome Measure Information:
Title
Multiple Sclerosis Functional Composite (MSFC)
Description
Composite score from Timed 25-Feet Walk Test (T25FWT), 9-Hole Peg Test (9HPT), Paced Auditory Serial Addition Test (PASAT)
Time Frame
Baseline, 24 weeks, after 1 year intervention, and again at 1 year follow up.
Title
Expanded Disability Status Scale (EDSS) score
Description
Disability status score assessed and registered by neurologist. The scale ranges from 0-10 in 0.5 unit increments representing higher levels of disability.
Time Frame
Baseline, after 1 year intervention, and again at 1 year follow up.
Other Pre-specified Outcome Measures:
Title
Functional capacity, Six-minute walk test (6MWT)
Description
Distance covered during a six-minute maximal walking test
Time Frame
Baseline, 24 weeks, after 1 year intervention, and again at 1 year follow up.
Title
Functional capacity, Six-spot-step-test (SSST)
Description
SSSt is a measure of walking ability, balance and coordination. Measured as the time to complete the six-spot course.
Time Frame
Baseline, 24 weeks, after 1 year intervention, and again at 1 year follow up.
Title
Functional capacity, Accelerometry
Description
Measurement of level of physical activity by wearing a accelerometer for 7 days at each timepoint. Measured in counts/min.
Time Frame
Baseline, 24 weeks, after 1 year intervention, and again at 1 year follow up.
Title
Aerobic capacity
Description
Maximal oxygen uptake test on bike ergometer, measured by indirect calorimetry.
Time Frame
Baseline, 24 weeks, after 1 year intervention, and again at 1 year follow up.
Title
Cognition, Symbol Digit Modality Test (SDMT)
Description
Assessment of cognitive function (processing speed), with a higher number of correct answers in the test representing better cognitive function.
Time Frame
Baseline, 24 weeks, after 1 year intervention, and again at 1 year follow up.
Title
Cognition, Paced Auditory Serial Addition Test (PASAT)
Description
Assessment of cognitive function (processing speed and memory), with a higher number of correct answers in the test representing better cognitive function.
Time Frame
Baseline, 24 weeks, after 1 year intervention, and again at 1 year follow up.
Title
Cognition, Selective Reminding Test (SRT)
Description
Assessment of cognitive function (memory), with a higher number of correct answers in the test representing better cognitive function.
Time Frame
Baseline, 24 weeks, after 1 year intervention, and again at 1 year follow up.
Title
Short Form Health Survey 36 (SF-36)
Description
Questionnaire assessing health status. The SF-36 consists of eight subscales, which are the weighted sums of the questions in their section. Each scale is directly transformed into a 0-100 scale on the assumption that each question carries equal weight. The lower the score the more disability. The higher the score the less disability.
Time Frame
Baseline, 24 weeks, after 1 year intervention, and again at 1 year follow up.
Title
Multiple Sclerosis Impact Scale 29 (MSIS-29)
Description
Questionnaire assessing the impact of the disease. 20 questions measure the physical impact, and 9 questions measure the psychological impact. Each question is scored from 1-5. A greater score is equal to a larger impact.
Time Frame
Baseline, 24 weeks, after 1 year intervention, and again at 1 year follow up.
Title
Multiple Sclerosis Walking Scale 12 (MSWS-12)
Description
Questionnaire assessing the impact of the disease on walking. Each question is scored from 1-5 and then summed and transformed to a 0-100 scale. Higher scores indicate a greater impact on walking.
Time Frame
Baseline, 24 weeks, after 1 year intervention, and again at 1 year follow up.
Title
Modified Fatigue Impact Scale (MFIS)
Description
Questionnaire assessing the effects of fatigue on physical, cognitive and psychosocial functioning. The score of the MFIS is the sum of the scores for the 21 items. A higher score represents a higher impact of fatigue, in general or in relation to one of the above mentioned areas.
Time Frame
Baseline, 24 weeks, after 1 year intervention, and again at 1 year follow up.
Title
Number of lesions
Description
Number of lesions, measured by MRI-scanning.
Time Frame
Baseline, 24 weeks, after 1 year intervention, and again at 1 year follow up.
Title
Lesion load
Description
Volume of lesions, measured by MRI-scanning.
Time Frame
Baseline, 24 weeks, after 1 year intervention, and again at 1 year follow up.
Title
Kurtosis
Description
MRI-measure of microstructural changes in the brain
Time Frame
Baseline, 24 weeks, after 1 year intervention, and again at 1 year follow up.
Title
Inflammation
Description
Blood samples will be analyzed for key inflammatory cytokines
Time Frame
Baseline, 24 weeks, after 1 year intervention, and again at 1 year follow up.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Signed consent
Definite diagnosis with Relapsing remitting multiple sclerosis (RRMS)
No more than 2 years since diagnosis
Expectedly able to carry out high intensity aerobic training
Able to transport themselves to and from training sessions
Exclusion Criteria:
Pregnancy
Dementia, alcohol abuse, or pacemaker
Metallic implants, hindering MRI-scans
Comorbidities hindering participation in high intensity aerobic training
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Morten Riemenschneider, MSc
Organizational Affiliation
Section for Sport Science, Department of Public Health, Aarhus University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Section for Sport Science, Department of Public Health, University of Aarhus
City
Aarhus
ZIP/Postal Code
8000
Country
Denmark
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
All data will be stored in The Danish National Archives after completion of the project, and data can be accessed through request to The Danish National Archives.
IPD Sharing Time Frame
The data will become available after completion of the project, expectedly January 2021. The Danish National Archives stores data without a time frame (forever).
IPD Sharing Access Criteria
Sharing of data can happen upon request to The Danish National Archives.
Citations:
PubMed Identifier
18970977
Citation
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Results Reference
background
PubMed Identifier
26346796
Citation
Ziemssen T, De Stefano N, Sormani MP, Van Wijmeersch B, Wiendl H, Kieseier BC. Optimizing therapy early in multiple sclerosis: An evidence-based view. Mult Scler Relat Disord. 2015 Sep;4(5):460-469. doi: 10.1016/j.msard.2015.07.007. Epub 2015 Jul 17.
Results Reference
background
PubMed Identifier
15794399
Citation
Patwardhan MB, Matchar DB, Samsa GP, McCrory DC, Williams RG, Li TT. Cost of multiple sclerosis by level of disability: a review of literature. Mult Scler. 2005 Apr;11(2):232-9. doi: 10.1191/1352458505ms1137oa.
Results Reference
background
PubMed Identifier
24485135
Citation
Wingerchuk DM, Carter JL. Multiple sclerosis: current and emerging disease-modifying therapies and treatment strategies. Mayo Clin Proc. 2014 Feb;89(2):225-40. doi: 10.1016/j.mayocp.2013.11.002.
Results Reference
background
PubMed Identifier
22206762
Citation
Elovaara I. Early treatment in multiple sclerosis. J Neurol Sci. 2011 Dec;311 Suppl 1:S24-8. doi: 10.1016/S0022-510X(11)70005-3.
Results Reference
background
PubMed Identifier
17881393
Citation
Dalgas U, Stenager E, Ingemann-Hansen T. Multiple sclerosis and physical exercise: recommendations for the application of resistance-, endurance- and combined training. Mult Scler. 2008 Jan;14(1):35-53. doi: 10.1177/1352458507079445. Epub 2007 Sep 19.
Results Reference
background
PubMed Identifier
28752800
Citation
Kjolhede T, Siemonsen S, Wenzel D, Stellmann JP, Ringgaard S, Pedersen BG, Stenager E, Petersen T, Vissing K, Heesen C, Dalgas U. Can resistance training impact MRI outcomes in relapsing-remitting multiple sclerosis? Mult Scler. 2018 Sep;24(10):1356-1365. doi: 10.1177/1352458517722645. Epub 2017 Jul 28.
Results Reference
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PubMed Identifier
33436475
Citation
Riemenschneider M, Hvid LG, Ringgaard S, Nygaard MKE, Eskildsen SF, Petersen T, Stenager E, Dalgas U. Study protocol: randomised controlled trial evaluating exercise therapy as a supplemental treatment strategy in early multiple sclerosis: the Early Multiple Sclerosis Exercise Study (EMSES). BMJ Open. 2021 Jan 12;11(1):e043699. doi: 10.1136/bmjopen-2020-043699.
Results Reference
derived
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Early Exercise Efforts in Multiple Sclerosis
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